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一名患有朱伯特综合征的儿科患者的麻醉管理:病例报告

Anesthetic management for a pediatric patient with joubert syndrome: A case report.

作者信息

Lee Yoon Sook, Kim Woon Young, Kim Kyoung Gun, Chang Moon Seok, Kim Jae Hwan, Park Young Cheol

机构信息

Department of Anesthesiology and Pain Medicine, Korea University Ansan Hospital, Korea University College of Medicine, Ansan, Korea.

出版信息

Korean J Anesthesiol. 2009 Jul;57(1):96-99. doi: 10.4097/kjae.2009.57.1.96.

Abstract

Joubert syndrome is a rare autosomal recessive condition in which there is complete or partial agenesis of the cerebellar vermis. The clinical features are hypotonia, ataxia, mental retardation, abnormal ocular movements, typical facial features and episodic tachypnea with alternating apnea. The abnormal respiratory pattern and hypotonia may be exacerbated by anesthetics, and especially, the apneic episodes may be prolonged by administering opioids. Joubert syndrome has been associated with various airway abnormalities such as a high and arched palate, a large or protruding tongue, laryngomalacia, a variable epiglottis and micrognathia. These abnormalities may cause difficulty with tracheal intubation. In this present case, direct laryngoscope-assisted, fiberscopic guided intubation was performed. This case is the first report of anesthetic management in a patient with Joubert syndrome and who underwent palatoplasty in Korea.

摘要

乔伯特综合征是一种罕见的常染色体隐性疾病,其小脑蚓部存在完全或部分发育不全。临床特征包括肌张力减退、共济失调、智力发育迟缓、异常眼球运动、典型面部特征以及伴有交替性呼吸暂停的发作性呼吸急促。麻醉剂可能会加重异常呼吸模式和肌张力减退,特别是,使用阿片类药物可能会延长呼吸暂停发作时间。乔伯特综合征与多种气道异常有关,如高拱腭、大舌头或突出舌头、喉软化、会厌形态各异以及小颌畸形。这些异常可能导致气管插管困难。在本病例中,实施了直接喉镜辅助下的纤维喉镜引导插管。该病例是韩国首例关于乔伯特综合征患者接受腭裂修复术的麻醉管理报告。

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